Canonical Allele Identifier: CA391692095
Community Standard Title: NM_001013703.4(EIF2AK4):c.2857C>A (p.Gln953Lys)
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39997054C>A , CM000677.2:g.39997054C>A GRCh38
NC_000015.9:g.40289255C>A , CM000677.1:g.40289255C>A GRCh37
NC_000015.8:g.38076547C>A NCBI36
NG_034053.1:g.67931C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001013703.4:c.2857C>A MANE Select NP_001013725.2:p.Gln953Lys
ENST00000263791.10:c.2857C>A MANE Select ENSP00000263791.5:p.Gln953Lys
NM_001013703.3:c.2857C>A NP_001013725.2:p.Gln953Lys
ENST00000263791.9:c.2857C>A ENSP00000263791.5:p.Gln953Lys
ENST00000558629.5:n.1774C>A
ENST00000560855.5:c.2189C>A
XM_005254392.1:c.2857C>A XP_005254449.1:p.Gln953Lys
XM_005254392.3:c.2857C>A XP_005254449.1:p.Gln953Lys
XM_011521599.1:c.2857C>A XP_011519901.1:p.Gln953Lys
XM_011521599.2:c.2857C>A XP_011519901.1:p.Gln953Lys
XM_011521600.1:c.2857C>A XP_011519902.1:p.Gln953Lys
XM_011521600.3:c.2857C>A XP_011519902.1:p.Gln953Lys
XM_017022219.2:c.2857C>A XP_016877708.1:p.Gln953Lys